Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
In this module, we learned about G protein function as a binary switch. G proteins have an intrinsic enzymatic ability to hydrolyze GTP to GDP + Pi. Why, then, would a cell need additional G protein controls like GEFs or GAPs? What advantages do you see this providing?
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by stepSolved in 2 steps
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Suppose a new patient, patient HLU, presents with fatigue and failure to thrive within a few days. Upon further investigation, it is discovered that HLU has hypoglycemia between feedings and lactic acidosis right after feeding. In addition, isoelectric focusing of the protein transferrin from his bloodstream, transferrin being a heavily glycosylated protein, reveals that HLU has erroneous N-linked glycosylation of transferrin. Biosynthesis of N-linked glycosylated glycoproteins require UDP-glucose and UDP-galactose for construction of the oligosaccharide that gets added to the protein in the endoplasmic reticulum. Muscle biopsy later in life reveals that he has a glycogen storage disease – there are excess amounts of normally structured glycogen in muscle cells. Early in life, he was subjected to the Beutler test and misdiagnosed with galactosemia because NADPH levels did not increase as readily as wild type patient upon administration of galactose. Which enzyme is deficient in…arrow_forwardTwo protein kinases, barley kinase and hops kinase, function sequentially in an intracellular signaling pathway. If either kinase contains a mutation that permanently inactivates it, no response is seen in cells when an extracellular signal is received. A mutation that permanently activates barley results in a response even when there is no extracellular signal. You characterize a double mutant in which hops has the inactivating mutation and barley has the activating mutation. You observe that a response is seen in the double mutants even in the absence of an extracellular signal. In the normal signaling pathway, does barley phosphorylate hops or does hops phosphorylate barley? Briefly explain your answer.arrow_forwardYou are in a research lab studying the function of the mutated form of a receptor called Protein X, which results in disruptive symptoms in human patients: extreme fatigue, low blood pressure, and dizziness among other symptoms that may be affecting the reproductive system. From detailed genetic studies, you have found that there is a mutation in the region where the Nuclear Localization Signal (NLS) of Protein X is, which may account for the symptoms seen in patients. What kind of receptor is Protein X most likely to be? Select one: O a. Steroid Family Receptor O b. GPCR Growth Hormone Receptor O d. Thyroid Hormone Receptorarrow_forward
- 1arrow_forwardWhich of the following dephosphorylates PI 3,4,5-trisphosphate, thereby blocking the activation of PKB/Akt?arrow_forwardNotch is an important transmembrane receptor that is present on the plasma membrane. Curiously, it possesses a proteolytic cleavage site and an NLS in its intracellular domain. In a protein fragment complementation experiment the Notch receptor was fused to the N-terminal portion of GFP on its intracellular domain. Another protein that is known to act in the nucleus to mediate the Notch signal following its activation was fused to the C-terminal region of GFP. When both are expressed in the same cell, GFP is observed in the nucleus. In 3-4 sentences provide an explanation that would account for the expression of GFP exclusively in the nucleus.arrow_forward
- When Hedgehog binds to Patched, this not only activates the signaling pathway but alsoactivates the receptor-mediated endocytosis of Patched, so there is less Patched on the plasmamembrane to inhibit Smoothened. a. Outline the steps of receptor-mediated endocytosis, including the roles for each proteininvolved. Hint: if your answer does not include the protein dynamin, you are notproviding enough detail. b. What will happen to Patched after it enters the cell via receptor-mediated endocytosis?Assume that Patched is not recycled back to the plasma membrane.arrow_forwardGenetic testing of a 29-month-old boy shows a mutation in the Phe residue at position 508 in the cystic fibrosis transmembrane conductance regulator (CFTCR) gene. Cultured skin fibroblasts from the boy contain an abnormal form of CFTCR protein bound to ubiquitin. Which of the following structures is the most likely site of elimination of these abnormal proteins in this patient? A) Endoplasmic reticulum B) Endosome C) Golgi complex D) Lysosome E) Proteasomearrow_forwardWhy are cytosolic hsp70 chaperone proteins required for import of proteins into mitochondria and chloroplasts, but not for translational import into the ER?arrow_forward
- RGS proteins accelerate the GAP activity of Gα subunits. What is the direct result of this GAP activity? - hydrolysis of GTP, resulting in a GDP-bound Gα - phosphorylation of GDP to GTP, resulting in a GTP-bound Gα - an exchange of GTP for GDP bound to Gα - an exchange of GDP for GTP bound to Gαarrow_forwardMutant tyrosine kinase signaling proteins are implicated in many types of human cancer. Hundreds of millions of dollars are required for the basic research and development of a new drug. Tyrosine kinase inhibitor drugs have been approved for cancer treatments by the U.S. Food and Drug Administration. What do you think would be some of the difficulties of finding these drugs given that similar kinases are active in normal cells? Do you think new medications of this type should be developed through government-sponsored research? Why or why not? If not, what alternatives do you propose?arrow_forwardFor each of the following statements regarding protein import into mitochondria, indicate whether it is likely to be true or false. [Select] into the mitochondria matrix. [Select] [Select] being translated [Select] unfolded state. The signal sequence is always retained after proteins are imported Chaperon proteins are needed for protein import into mitochondria ✓ Imported proteins cross the mitochondrial membrane while it is still Proteins imported into mitochondria cross the membrane inarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:PEARSON
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Anatomy & Physiology
Biology
ISBN:9781259398629
Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:9780815344322
Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:9781260159363
Author:Martin, Terry R., Prentice-craver, Cynthia
Publisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Biology
ISBN:9781260231700
Author:Sylvia S. Mader, Michael Windelspecht
Publisher:McGraw Hill Education